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N-amino-N-butylformamide

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Identification
Molecular formula
C5H12N2O
CAS number
759-77-1
IUPAC name
N-amino-N-butyl-formamide
State
State

N-amino-N-butylformamide is a liquid at room temperature.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
209.80
Boiling point (Kelvin)
482.95
General information
Molecular weight
116.16g/mol
Molar mass
116.1580g/mol
Density
0.9420g/cm3
Appearence

N-amino-N-butylformamide appears as a colorless to pale yellow liquid. It may have a weak, ammonia-like odor due to its amide and amine functional groups.

Comment on solubility

Solubility of N-amino-N-butyl-formamide

N-amino-N-butyl-formamide, with the chemical formula C5H12N2O, is known for its interesting solubility properties. This compound displays considerable solubility in various solvents due to its polar functional groups. Here are some key points regarding its solubility characteristics:

  • Water Solubility: N-amino-N-butyl-formamide is generally quite soluble in water, thanks to the presence of the amine and carbonyl groups which can engage in hydrogen bonding.
  • Organic Solvents: It also exhibits solubility in polar organic solvents like alcohols and dimethyl sulfoxide (DMSO), enhancing its versatility in chemical applications.
  • Temperature Dependency: The solubility can be affected by temperature, where increased temperature may lead to higher solubility in both water and organic solvents.

As a rule of thumb, compounds with functional groups capable of hydrogen bonding tend to be more soluble in polar solvents compared to those that are non-polar. The structural features of N-amino-N-butyl-formamide align with this principle, making it a compound of interest in various research and industrial applications.

Interesting facts

Interesting Facts About N-amino-N-butyl-formamide

N-amino-N-butyl-formamide, often referred to in academic and industrial circles as a versatile organic compound, has a unique structure that opens the door to various applications and intriguing characteristics. Below are several fascinating aspects of this compound:

  • Biological Significance: N-amino-N-butyl-formamide has been studied for its potential role in biological systems, acting as a substrate in various biochemical pathways.
  • Synthetic Applications: This compound is essential in the synthesis of other chemicals, showcasing its versatility in the organic chemistry landscape. It can be utilized as an intermediate in the production of pharmaceuticals and agrochemicals.
  • Chemical Reactivity: N-amino-N-butyl-formamide contains both amine and formamide functional groups, making it highly reactive. This reactivity enables it to participate in diverse reactions, from Michael additions to condensation reactions.
  • Environmental Impact: As with many organic compounds, understanding the environmental impact of N-amino-N-butyl-formamide is crucial. Studies into its biodegradability and potential toxicity inform safe handling practices and regulatory compliance.
  • Research Potential: Ongoing research into N-amino-N-butyl-formamide indicates that it may have further unexplored properties that can be harnessed in advanced material science and nanotechnology.

In the world of chemistry, compounds like N-amino-N-butyl-formamide remind us of the intricate connections between molecular structure and chemical behavior. As noted by researchers, "The pathways of organic synthesis are often paved with unexpected reactions and configurations." This highlights the ongoing necessity for chemists to explore and document these unconventional compounds to unlock new possibilities for innovation.


Synonyms
N-n-butyl-n-formylhydrazine
16120-70-0
FORMIC ACID, 1-BUTYLHYDRAZIDE
2D4RL3QE57
N-amino-N-butylformamide
BFH
N-butylformic hydrazide
BRN 3043748
N-Butyl-N-formylhydrazine
UNII-2D4RL3QE57
Formic acid N-butyl-hydrazide
SCHEMBL7166809
SCHEMBL7456117
DTXSID8020208
Hydrazinecarboxaldehyde, 1-butyl-
1-BUTYLHYDRAZINECARBOXALDEHYDE
BUTYL-N-FORMYLHYDRAZINE, N-N-
Q63088105